Mosaic 46,XY/92,XXYY,del(5)(q13 q34) in an adult lymphoblastic leukemia

Leuk Res. 1991;15(7):651-3. doi: 10.1016/0145-2126(91)90035-r.

Abstract

Usually the chromosome anomalies encountered in ALL are modal number abnormalities (hyperdiploidy or hypodiploidy) and structural anomalies such as t(8;14), t(11;14), t(9;22), t(1;19) and del(6p). The 5q- syndrome is mainly associated with myelodysplastic syndromes and with ANLL (M1, M2, M3). We report the case of a patient presenting with a mosaic karyotype 46,XY/92,XXYY,del(5)(q13 q34) in the following proportion 1/3 normal mitoses and 2/3 tetraploid mitoses.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 5 / physiology
  • Humans
  • Karyotyping
  • Male
  • Ploidies*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics*
  • Sex Chromosome Aberrations / genetics
  • X Chromosome / physiology
  • Y Chromosome / physiology